Basis of Muscle Dysfunction in Malignant Hyperthermia and Central Core Disease

恶性高热和中央核心疾病中肌肉功能障碍的基础

• 批准号: 8608998
• 负责人: Robert T Dirksen
• 金额: $ 65.84万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-04-01 至 2016-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8608998
• 关键词: AMP-activated protein kinase kinase; Acetylcysteine; Aging; Aminoimidazole Carboxamide; Anesthetics; Antioxidants; Automobile Driving; Binding; Calcium; Central Core Myopathy; Cessation of life; Contracture; Coupled; Coupling; Dantrolene; Development; Diet; Dihydropyridine Receptors; Disease; Dominant-Negative Mutation; Exercise; Exhibits; FDA approved; Fatty acid glycerol esters; Functional disorder; Genes; Goals; Heating; Human; Intervention; Life; Ligands; Link; Malignant hyperpyrexia due to anesthesia; Metabolism; Mitochondria; Modeling; Mus; Muscle; Muscle function; Mutation; Myopathy; Outcome; Oxidative Stress; Paralysed; Pathway interactions; Process; Production; Proteins; Research; Research Personnel; Rhabdomyolysis; Ribonucleotides; Role; RyR1; Ryanodine Receptor Calcium Release Channel; Sarcoplasmic Reticulum; Skeletal Muscle; Symptoms; Tacrolimus Binding Protein 1A; Tacrolimus Binding Proteins; Technology; Temperature; Testing; Therapeutic Intervention; Work; base; congenital myopathy; efficacy testing; flexibility; improved; in vivo; innovation; mouse model; novel therapeutic intervention; prevent; public health relevance; response; therapy design; treatment strategy; voltage

DESCRIPTION (provided by applicant): Mutations in the RYR1 gene underlie several debilitating, life-threatening muscle diseases. In this application we are proposing to use a mouse model with a knockin mutation into RyR1 (Y524S) that has features of three of these disorders: malignant hyperthermia (MH) heat/exercise-induced exertional rhabdomyolysis (ER) and central core disease (CCD). Our long term goals are to define the mechanisms that underlie the decline in muscle function associated with these diseases and to develop new interventions. Our overall working hypothesis for the current proposal the Y524S mutation in RyR1 increases the temperature sensitivity of both excitation-contraction coupling (ECC) and RyR1 Ca2+ leak, producing the MH response and driving oxidative stress and mitochondrial destruction that leads to the myopathy. Our specific aims are to: 1) Elucidate the role of Ca2+ influx via CaV1.1 in the MH response and the development of the myopathy; 2) Delineate the mechanisms of core formation in YS mice; 3) Define the mechanism by which an activator (AICAR) of the energy sensing kinase AMPK prevents the MH response and evaluate AICAR's ability to slow the development of the myopathy in YS mice; and 4) Define the mechanism by which a non-immunosuppressive ligand for the protein FKBP12 prevents the MH response and evaluate SLF's effect on the myopathy in YS mice. The proposed work is highly significant because we directly couple the delineation of pathways underlying disease processes with the development of novel therapeutic interventions that have distinct mechanisms of action, allowing for some flexibility to tailor treatment strategies to different mutations associated with MH and CCD. The proposed research is innovative because of: 1) paradigm shifting hypotheses; 2) unique mouse models, 3) cutting edge technologies, and 4) therapeutic interventions never previously proposed as treatments for MH or other RyR1-linked myopathies.

描述(申请人提供)：RYR1基因突变是几种衰弱的、危及生命的肌肉疾病的基础。在这项应用中，我们建议使用RyR1(Y524S)敲击突变的小鼠模型，该模型具有以下三种疾病的特征：恶性高热(MH)、热/运动诱导的劳力性横纹肌溶解(ER)和中枢性核心病(CCD)。我们的长期目标是确定与这些疾病相关的肌肉功能下降的基础机制，并开发新的干预措施。我们对当前建议的总体工作假设是，RyR1的Y524S突变增加了兴奋收缩偶联(ECC)和RyR1钙泄漏的温度敏感性，产生MH反应，并驱动氧化应激和线粒体破坏，从而导致肌病。我们的具体目标是：1)阐明通过CaV1.1进行的钙离子内流在MH反应和肌病发展中的作用；2)描述YS小鼠核心形成的机制；3)确定能量感应激酶AMPK的激活剂(AICAR)阻止MH反应的机制并评估AICAR减缓YS小鼠肌病发展的能力；以及4)确定非免疫抑制配体FKBP12阻止MH反应的机制，并评价SLF对YS小鼠肌病的影响。拟议的工作具有非常重要的意义，因为我们直接将疾病过程潜在途径的描绘与具有不同作用机制的新型治疗干预措施的开发结合在一起，允许有一定的灵活性来针对与MH和CD相关的不同突变定制治疗策略。这项拟议的研究具有创新性，因为：1)范式转换假说；2)独特的小鼠模型；3)尖端技术；4)以前从未被提出用于治疗MH或其他RyR1相关肌病的治疗干预措施。